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11 часов назад

Archives Coordinator (Clinical Research)

Формат работы
onsite
Тип работы
fulltime
Грейд
junior
Английский
b2
Страна
UK
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Archives Coordinator (Clinical Research): Managing controlled documents and electronic archives for a Quality Assurance department with an accent on accurate cataloguing, secure retention, retrieval, and regulatory compliance. Focus on preparing records for offsite storage, monitoring archive lifecycle metrics, supporting audits and CAPAs, and improving quality processes.

Location: Onsite in York, United Kingdom; Monday–Friday, 8:00 AM–4:00 PM, 37.5 hours per week

Company

hirify.global provides laboratory and clinical research services.

What you will do

  • Manage the controlled document and electronic archive lifecycle, including cataloguing, retrieval, retention, transfer, and destruction monitoring.
  • Archive controlled documents, forms, templates, study documentation, laboratory source data, and other clinical trial records.
  • Perform quality checks and maintain records for documents held onsite and in commercial offsite archives.
  • Run reports and monitor compliance with storage duration, record descriptors, retention periods, and destruction dates.
  • Support audits, quality metrics, customer complaints, Quality Issues, CAPAs, audit responses, and site training.
  • Contribute to Lean/Six Sigma, continuous improvement, and collaboration across the global archiving network.

Requirements

  • High school diploma or equivalent, or five GCSE grades C or above including Maths, English, and Science.
  • At least one year of experience in a relevant role.
  • Strong organizational, written and verbal communication, and time management skills.
  • Ability to work independently and as part of a team.
  • Ability to perform moderate physical work, including frequent standing and walking and lifting up to 50 lbs.

Nice to have

  • Experience in laboratory Quality Assurance, a pharmaceutical organization, or a Clinical Research Organization.
  • Knowledge of and experience applying Good Clinical Practice guidance.

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